Uuden syövän vastaisten lääkkeiden yhdistelmän testaaminen potilailla, joilla on äskettäin diagnosoitu Ewing-sarkooma, jolla on syöpä, joka on levinnyt muihin kehon osiin
Vinkristiini-irinotekaanirregorafenibin satunnaistettu vaihe 2/3 yhdessä vinkristiinidoksorubisiinin syklofosfamidin (VDC) ja ifosfamidi-etoposidin (IE) kanssa potilailla, joilla on äskettäin diagnosoitu metastaattinen uinaus
This phase II/III trial compares the effect of vincristine, irinotecan, and regorafenib (VIrR) in combination with vincristine, doxorubicin, cyclophosphamide (VDC), ifosfamide and etoposide (IE) to usual treatment with VDC/IE for the treatment of newly diagnosed Ewing sarcoma or other round cell sarcomas that have spread from where they first started (primary site) to other places in the body (metastatic). Vincristine is in a class of medications called vinca alkaloids. It works by stopping tumor cells from growing and dividing and may kill them. Irinotecan is in a class of antineoplastic medications called topoisomerase I inhibitors. It blocks a certain enzyme needed for cell division and deoxyribonucleic acid (DNA) repair and may kill tumor cells. Regorafenib, a type of kinase inhibitor and a type of antiangiogenesis agent, blocks certain proteins, which may help keep tumor cells from growing. It may also prevent the growth of new blood vessels that tumors need to grow. Doxorubicin is in a class of medications called anthracyclines. Doxorubicin damages the cell's DNA and may kill tumor cells. It also blocks a certain enzyme needed for cell division and DNA repair. Cyclophosphamide is in a class of medications called alkylating agents. It works by damaging the cell's DNA and may kill tumor cells. It may also lower the body's immune response. Ifosfamide, a type of alkylating agent and a type of antimetabolite, attaches to DNA in cells and may kill tumor cells. Etoposide is in a class of medications known as podophyllotoxin derivatives. It blocks a certain enzyme needed for cell division and DNA repair and may kill tumor cells. Giving VIrR/VDC/IE may be more effective than usual treatment with VDC/IE in treating patients with newly diagnosed metastatic Ewing sarcoma or other round cell sarcomas.
Tutkimuksen yleiskatsaus
Tila
Ehdot
- Metastaattinen Ewing-sarkooma
- CIC-uudelleenjärjestetty sarkooma
- Pyöreäsoluinen sarkooma EWSR1-ei-ETS-fuusion kanssa
- Metastaattinen korkealaatuista sarkoomaa
- Sarkooma BCOR -geneettisten muutosten kanssa
- Metastaattinen erottamaton pyöreän solun sarkooma
- Metastaattinen erottamaton sarkooma, jota ei muuten määritetty
Interventio / Hoito
- Lääke: Cyclophosphamide
- Lääke: Doxorubicin Hydrochloride
- Lääke: Vincristine Sulfate
- Menettely: Computed Tomography
- Menettely: Magnetic Resonance Imaging
- Muut: Questionnaire Administration
- Menettely: Bone Marrow Aspiration
- Menettely: Bone Marrow Biopsy
- Lääke: Etoposide
- Lääke: Ifosfamide
- Lääke: Irinotecan Hydrochloride
- Säteily: Radiation Therapy
- Menettely: Echocardiography Test
- Menettely: Surgical Procedure
- Muut: Fludeoxyglucose F-18
- Menettely: Positron Emission Tomography
- Menettely: Biopsy Procedure
- Menettely: Biospecimen Collection
- Lääke: Regorafenib
Yksityiskohtainen kuvaus
PRIMARY OBJECTIVE:
I. To determine if the event-free survival (EFS) in patients with newly diagnosed metastatic Ewing sarcoma is improved when treated with vincristine-irinotecan-regorafenib (VIrR) after initial treatment with vincristine-doxorubicin-cyclophosphamide (VDC) and ifosfamide-etoposide (IE) compared to patients treated with 17 cycles of interval compressed VDC and IE chemotherapy.
SECONDARY OBJECTIVES:
I. To compare the overall survival (OS) of patients with newly diagnosed metastatic Ewing sarcoma treated with VDC/IE/VIrR versus VDC/IE.
II. To compare the toxicity profile of VDC/IE/VIrR to VDC/IE in patients with newly diagnosed metastatic Ewing sarcoma, using both investigator-reported and patient-reported Common Terminology Criteria for Adverse Events (CTCAE).
III. To describe the feasibility and toxicity of augmented dose radiotherapy with 64.8 Gy as local control for patients with newly diagnosed metastatic Ewing sarcoma with large primary tumors.
IV. To prospectively validate that circulating tumor-derived DNA (ctDNA) levels greater than or equal to 5% at the time of diagnosis are associated with increased risk of EFS-event for patients with newly diagnosed metastatic Ewing sarcoma.
V. To prospectively validate that elevated ctDNA levels greater than or equal to 0.5% burden following one cycle of chemotherapy are associated with increased risk of EFS-event for patients with newly diagnosed metastatic Ewing sarcoma.
EXPLORATORY OBJECTIVES:
I. To estimate 1- and 2-year EFS and response rate for patients with newly diagnosed, eligible metastatic round cell sarcomas other than Ewing sarcoma.
II. To characterize the change in fludeoxyglucose F-18 (FDG)-positron emission tomography (PET) imaging response of primary disease site at the end of Induction chemotherapy and its association with EFS.
III. To explore distinguishing histologic attributes of Ewing sarcoma and round cell sarcomas that mimic Ewing sarcoma.
IV. To collect bone marrow and tissue samples to bank for future research. V. To explore other ctDNA predictor variables, time points, and potential association with EFS in patients with newly diagnosed metastatic Ewing sarcoma.
VI. To estimate the frequency of selected toxicities by Patient Reported Outcomes (PRO)-CTCAE and symptom bother by Functional Assessment of Cancer Therapy General Questionnaire (FACT-G) and to evaluate if these findings are associated with duration of protocol therapy and treatment arm.
OUTLINE:
INDUCTION: Patients receive vincristine intravenously (IV) on days 1 and 8, doxorubicin IV over 3-15 minutes on days 1 and 2, and cyclophosphamide IV over 30-60 minutes on day 1 of cycles 1, 3 and 5. Patients also receive ifosfamide IV over 1 hour and etoposide IV over 1 hour on days 1-5 of cycles 2, 4 and 6. Cycles repeat every 14 days for up to 6 cycles in the absence of disease progression or unacceptable toxicity. Patients then undergo surgery or radiation therapy per investigator choice.
CONSOLIDATION I: Patients receive vincristine IV on days 1 and 8, doxorubicin IV over 3-15 minutes on days 1 and 2, and cyclophosphamide IV over 30-60 minutes on day 1 of cycles 1 and 2. Patients also receive ifosfamide IV over 1 hour and etoposide IV over 1 hour on days 1-5 of cycles 3 and 4. Cycles repeat every 14 days for up to 4 cycles in the absence of disease progression or unacceptable toxicity.
CONSOLIDATION II: After 10 cycles of therapy, patients with Ewing Sarcoma are randomized to 1 of 2 regimens. Patients with a diagnosis of other eligible metastatic round cell sarcomas are assigned to Regimen A.
REGIMEN A: Patients receive vincristine IV on days 1 and 8 and cyclophosphamide IV over 30-60 minutes on day 1 of cycles 1, 3, 5 and 7. Patients also receive ifosfamide IV over 1 hour and etoposide IV over 1 hour on days 1-5 of cycles 2, 4 and 6. Cycles repeat every 14 days for up to 7 cycles in the absence of disease progression or unacceptable toxicity. After systemic therapy completed, patients undergo metastatic site radiation therapy.
REGIMEN B: Patients receive vincristine IV on days 1 and 8 and irinotecan IV over 90 minutes on days 1-5 of each cycle. Patients also receive regorafenib orally (PO) on days 8-14 or 15-21 of cycle 1, and then on days 8-21 of cycles thereafter. Cycles repeat every 21 days for up to 6 cycles in the absence of disease progression or unacceptable toxicity. After systemic therapy completed, patients undergo metastatic site radiation therapy.
Additionally, patients undergo blood sample collection, echocardiography, magnetic resonance imaging (MRI), computed tomography (CT), chest CT, and/or FDG-PET throughout the study. Patients may also undergo optional collection of tumor tissue and/or bone marrow aspiration and biopsy on study.
After completion of study treatment, patients are followed every 3 months for years 1 and 2, every 6 months for years 3 and 4 then every 12 months for years 5-10.
Opintotyyppi
Ilmoittautuminen (Todellinen)
Vaihe
- Vaihe 2
- Vaihe 3
Yhteystiedot ja paikat
Opiskelupaikat
-
-
Alabama
-
Birmingham, Alabama, Yhdysvallat, 35233
- Children's Hospital of Alabama
-
-
Hawaii
-
Honolulu, Hawaii, Yhdysvallat, 96826
- Kapiolani Medical Center for Women and Children
-
-
Illinois
-
Chicago, Illinois, Yhdysvallat, 60611
- Lurie Children's Hospital-Chicago
-
Peoria, Illinois, Yhdysvallat, 61637
- OSF Children's Hospital of Illinois
-
-
Pennsylvania
-
Philadelphia, Pennsylvania, Yhdysvallat, 19134
- Saint Christopher's Hospital for Children
-
-
South Carolina
-
Columbia, South Carolina, Yhdysvallat, 29203
- Prisma Health Richland Hospital
-
Greenville, South Carolina, Yhdysvallat, 29605
- BI-LO Charities Children's Cancer Center
-
-
Tennessee
-
Knoxville, Tennessee, Yhdysvallat, 37916
- East Tennessee Childrens Hospital
-
-
Osallistumiskriteerit
Kelpoisuusvaatimukset
Opintokelpoiset iät
Hyväksyy terveitä vapaaehtoisia
Sukupuolet, jotka voivat opiskella
Kuvaus
Inclusion Criteria:
-
All patients must be enrolled on APEC14B1 and consented to the Molecular Characterization Initiative (Part A) prior to enrollment and treatment on AEWS2431
-
Patients must be ≥ 12 months to ≤ 50 years of age at time of enrollment
-
Newly diagnosed Ewing sarcoma and other round cell sarcomas as follows. For the purposes of eligibility, the following pathology diagnoses are eligible and molecular confirmation is not required to enroll:
- Histologically confirmed Ewing sarcoma
- Suspected Ewing sarcoma with molecular confirmation pending
- Suspected high grade round cell sarcomas/sarcomas with eligible molecular alterations, pending molecular confirmation
- Round cell sarcoma consistent with Ewing sarcoma
- Round cell sarcoma not otherwise specified
- Round cell sarcoma
- Round cell sarcomas with EWSR1-non-ETS fusion
- CIC-rearranged sarcoma
- Sarcoma with BCOR genetic alterations
-
Patients with the following pathologic diagnoses that are known to contain EWSR1 or FUS fusions are not eligible:
- Angiomatoid fibrous histiocytoma
- Extraskeletal myxoid chondrosarcoma
- Desmoplastic small round cell tumor
- Clear cell sarcoma
- Myxoid liposarcoma
-
If clinical molecular testing that reports both fusion partners has been successfully completed by the site prior to enrollment, patients may only enroll if that testing reported one of the eligible fusions
-
All patients must have evidence of distant metastatic disease. Biopsy of metastatic sites is not required. For this study, distant metastatic disease is defined as one or more of the following:
-
Lesions which are discontinuous from the primary tumor, are not regional lymph nodes, and do not share a bone or body cavity with the primary tumor. Skip lesions in the same bone as the primary tumor do not constitute metastatic disease. Skip lesions in an adjacent bone are considered bone metastasis. If there is any doubt whether lesions are metastatic, a biopsy of those lesions should be performed
-
Contralateral pleural effusion and/or contralateral pleural nodules
-
Distant lymph node involvement
-
Patients with pulmonary nodules are considered to have metastatic disease if the patient has:
- Solitary nodule ≥ 0.5 cm or multiple nodules of ≥ 0.3 cm unless lesion is biopsied and negative for tumor
- Patients with solitary nodule < 0.5 cm or multiple nodules < 0.3 cm are not considered to have lung metastasis unless biopsy documents tumor
-
Bone marrow metastatic disease (bone marrow disease) is based on morphologic evidence of Ewing sarcoma based on hematoxylin and eosin (H&E) stains. In the absence of morphologic evidence of marrow involvement on H&E, patients with bone marrow involvement detected ONLY by flow cytometry, reverse transcriptase-polymerase chain reaction (RT-PCR), fluorescence in situ hybridization (FISH), immunohistochemistry or PET-CT will NOT be considered to have clinical bone marrow involvement for the purposes of this study
-
-
Creatinine clearance or radioisotope glomerular filtration rate (GFR) ≥ 50 mL/min/1.73 m^2 or serum creatinine based on age/sex as follows:
- Age: 1 to < 2 years: Male 0.6; female 0.6
- Age: 2 to < 6 years: Male 0.8; female 0.8
- Age: 6 to < 10 years: Male 1; female 1
- Age: 10 to < 13 years: Male 1.2; female 1.2
- Age: 13 to < 16 years: Male 1.5; female 1.4
- Age: ≥ 16 years: Male 1.7; female 1.4 OR
- A 24-hour urine creatinine clearance ≥ 50 mL/min/1.73 m^2 OR
- A GFR ≥ 50 mL/min/1.73 m^2. GFR must be performed using direct measurement with a nuclear blood sampling method OR direct small molecule clearance method (iothalamate or other molecule per institutional standard)
-
Total bilirubin ≤ 1.5 x upper limit of normal (ULN) for age
-
Serum glutamic pyruvic transaminase (SGPT) (alanine aminotransferase [ALT]) ≤ 3 x ULN for age (except for patients with liver metastasis who may enroll if ALT ≤ 5 times ULN for age)
- Note: For the purpose of this study, the ULN for SGPT (ALT) has been set to the value of 45 U/L
-
Shortening fraction of ≥ 27% by echocardiogram, or ejection fraction of ≥ 50% by echocardiogram
-
No known congenital QT syndrome
-
No known family history of congenital QT syndrome
-
Patients with known history or current symptoms of cardiac disease, or history of treatment with cardiotoxic agents, should have a clinical risk assessment of cardiac function using the New York Heart Association Functional Classification. To be eligible for this trial, patients should be class II or better
-
Known HIV-infected patients on effective anti-retroviral therapy with undetectable viral load within 6 months are eligible for this trial
Exclusion Criteria:
-
Patients with regional node involvement as their only site of disease beyond the primary tumor
-
Patients whose primary tumors arise in the intra-dural soft tissue (e.g., brain and spinal cord)
- Note: metastatic disease is allowable
-
Patients with known Charcot-Marie-Tooth disease
-
Patients who have had complete or partial resection of the primary tumor at initial diagnosis will only be eligible if adequate imaging (CT or MRI for most primary tumor sites) was obtained prior to surgery
-
Patients who have received prior chemotherapy for current diagnosis, except for patients who have started cycle 1 VDC post-consent and within the timelines allowed for
-
Patients who have received prior radiation therapy for current diagnosis
-
Patients previously treated with a multitargeted tyrosine kinase inhibitor
-
History of organ allograft (including allogeneic bone marrow transplant)
-
Known hypersensitivity to regorafenib
-
Active or chronic hepatitis B or C, or chronic hepatitis B or C requiring treatment with antiviral therapy
-
Patients receiving strong CYP3A4 inducers or strong CYP3A4 inhibitors
-
Female patients who are pregnant since fetal toxicities and teratogenic effects have been noted for several of the study drugs. A pregnancy test is required for female patients of childbearing potential
-
Lactating females who plan to breastfeed their infants
-
Females of childbearing potential must agree to either practice medically accepted highly-effective methods of contraception or abstain from heterosexual intercourse for the duration of the protocol therapy through 12 months after the last dose of cyclophosphamide or ifosfamide, 6 months after the last dose of doxorubicin, etoposide, and irinotecan, and 7 months after the last dose of regorafenib, whichever is longer
-
Male patients with female partners of childbearing potential must agree to either practice a medically accepted highly-effective methods of contraception or abstain from heterosexual intercourse for the duration of the protocol therapy through 6 months after the last dose of doxorubicin and ifosfamide, 4 months after the last dose of cyclophosphamide, etoposide and regorafenib, and 3 months after the last dose of irinotecan, whichever is longer
-
All patients and/or their parents or legal guardians must sign a written informed consent
-
All institutional, Food and Drug Administration (FDA), and National Cancer Institute (NCI) requirements for human studies must be met
Opintosuunnitelma
Miten tutkimus on suunniteltu?
Suunnittelun yksityiskohdat
- Ensisijainen käyttötarkoitus: Hoito
- Jako: Satunnaistettu
- Inventiomalli: Rinnakkaistehtävä
- Naamiointi: Ei mitään (avoin tarra)
Aseet ja interventiot
Osallistujaryhmä / Arm |
Interventio / Hoito |
|---|---|
|
Active Comparator: Regimen A (VDC/IE)
See Detailed description |
Given IV
Muut nimet:
Given IV
Muut nimet:
Given IV
Muut nimet:
Undergo CT
Muut nimet:
Undergo MRI
Muut nimet:
Ancillary studies Undergo bone marrow aspiration and biopsy Undergo bone marrow aspiration and biopsy
Muut nimet:
Given IV
Muut nimet:
Given IV
Muut nimet:
Undergo radiation
Muut nimet:
Undergo echocardiography
Muut nimet:
Undergo surgery
Muut nimet:
Given FDG
Muut nimet:
Undergo FDG PET
Muut nimet:
Undergo bone marrow aspiration and biopsy
Muut nimet:
Undergo tissue and/or blood sample collection
Muut nimet:
|
|
Kokeellinen: Regimen B (VIrR/VDC/IE)
See Detailed Description |
Given IV
Muut nimet:
Given IV
Muut nimet:
Given IV
Muut nimet:
Undergo CT
Muut nimet:
Undergo MRI
Muut nimet:
Ancillary studies Undergo bone marrow aspiration and biopsy Undergo bone marrow aspiration and biopsy
Muut nimet:
Given IV
Muut nimet:
Given IV
Muut nimet:
Given IV
Muut nimet:
Undergo radiation
Muut nimet:
Undergo echocardiography
Muut nimet:
Undergo surgery
Muut nimet:
Given FDG
Muut nimet:
Undergo FDG PET
Muut nimet:
Undergo bone marrow aspiration and biopsy
Muut nimet:
Undergo tissue and/or blood sample collection
Muut nimet:
Given PO
Muut nimet:
|
Mitä tutkimuksessa mitataan?
Ensisijaiset tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
|
Time to event-free survival (EFS) post-Consolidation I (C1)
Aikaikkuna: From randomization to progression or relapse, diagnosis of a second malignant neoplasm, death, or last patient contact, whichever occurs first, assessed up to 10 years
|
Analysis will be done by associating each patient's outcome with the individual's randomized treatment assignment. The associated statistical tests will be stratified according to grouping. |
From randomization to progression or relapse, diagnosis of a second malignant neoplasm, death, or last patient contact, whichever occurs first, assessed up to 10 years
|
Toissijaiset tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
|
Overall survival-C1
Aikaikkuna: From randomization to death or last patient contact, whichever occurs first, assessed up to 10 years
|
The stratified one-sided logrank test will be the primary statistical methodology for assessing the null statistical hypothesis. |
From randomization to death or last patient contact, whichever occurs first, assessed up to 10 years
|
|
Incidence of adverse events
Aikaikkuna: Up to 30 days after last dose of study treatment
|
Toxicity will be coded according to the Common Terminology Criteria for Adverse Events (CTCAE) version (v) 5. |
Up to 30 days after last dose of study treatment
|
|
Feasibility of augmented dose radiotherapy (ADRT) as local control
Aikaikkuna: Up to point of radiation therapy (RT) termination
|
The actual RT delivered will be compared with the treatment plan until the point of RT termination as assessed by central review. Will consider ADRT to be feasible to deliver if there is evidence that the patient-specific probability of feasibility-failure is less than 15%. |
Up to point of radiation therapy (RT) termination
|
|
Toxicity of ADRT as local control
Aikaikkuna: Up to 30 days after ADRT is completed
|
Will be evaluated using CTCAE v 5. |
Up to 30 days after ADRT is completed
|
|
Validation of circulating tumor-derived deoxyribonucleic acid (ctDNA) levels greater than or equal to 5% at the time of diagnosis are associated with increased risk of EFS-event
Aikaikkuna: At time of diagnosis
|
Will compare the risk for EFS-event from enrollment for groups of patients defined by percent ctDNA at diagnosis using a two-sided logrank test. |
At time of diagnosis
|
|
Validation of ctDNA levels greater than or equal to 0.5% following one cycle of chemotherapy are associated with increased risk of EFS-event
Aikaikkuna: Following one cycle of chemotherapy at induction (cycle length = 14 days)
|
Will compare the risk for EFS-event from enrollment for groups of patients defined by percent ctDNA at induction cycle 1 day 14 using a two-sided logrank test. |
Following one cycle of chemotherapy at induction (cycle length = 14 days)
|
Muut tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
|
EFS and response rate for patients with newly diagnosed eligible metastatic round cell sarcomas
Aikaikkuna: At 1 and 2 years
|
The 95% confidence bounds will be calculated according to the complementary log-log transformation. Will report the 1-, 2- and 3-year estimate EFS probabilities as well as the confidence intervals. |
At 1 and 2 years
|
|
Change in fludeoxyglucose F-18 positron emission tomography imaging response of primary disease site and its association with EFS
Aikaikkuna: At the end of 6 cycles of induction chemotherapy (cycle length = 14 days)
|
Will calculate the percent change in standardized uptake value (SUV). Will fit a Cox proportional hazards regression model for hazard of EFS-event with percent change in SUV included as an independent variable. Nonlinearity will be formally tested using a two degree of freedom Wald test of size 0.05 for the null hypothesis. The functional form of the relationship between hazard of EFS-event and percent change in SUV will be explored by plotting the model-predicted hazard on the logarithmic scale against percent change in SUV with 95% confidence bands. This plot will be examined for natural inflection points in the curve representing potentially informative categories of percent change in SUV. If the p-value for this test is not significant at the 0.05 level, will remove the nonlinear spline terms refitting the model with linear percent change in SUV, and will report the associated hazard ratio and 95% confidence interval. |
At the end of 6 cycles of induction chemotherapy (cycle length = 14 days)
|
|
Histologic attributes of Ewing sarcoma and round cell sarcomas that mimic Ewing sarcoma
Aikaikkuna: Up to 10 years
|
Qualitative characteristics will be quantified with the observed proportion in each category and the associated confidence interval. The sample mean, median, standard deviation, 25th percentile and 75th percentile will be used to characterize the distribution of the quantitative characteristics. |
Up to 10 years
|
|
ctDNA burden as a continuous variable
Aikaikkuna: Up to following two cycles of chemotherapy (cycle length = 14 days)
|
Will evaluate differences in hazard of EFS event by ctDNA as a continuous variable modeled as a restricted cubic spline in a proportional hazards regression model. |
Up to following two cycles of chemotherapy (cycle length = 14 days)
|
|
ctDNA burden prior to induction cycle 3
Aikaikkuna: Following two cycles of chemotherapy (cycle length = 14 days)
|
Will evaluate whether there is an increased risk of EFS event by ctDNA burden dichotomized at 0.5% prior to induction cycle 3 using a two-sided logrank test. |
Following two cycles of chemotherapy (cycle length = 14 days)
|
|
Change in ctDNA burden from diagnosis to local control
Aikaikkuna: Up to following two cycles of chemotherapy (cycle length = 14 days)
|
Will evaluate differences in hazard of EFS event by change in ctDNA burden as a continuous variable modeled as a restricted cubic spline in a proportional hazards regression model. |
Up to following two cycles of chemotherapy (cycle length = 14 days)
|
|
ctDNA burden after consolidation 1
Aikaikkuna: Up to 6 months after completion of planned therapy
|
Will evaluate whether there is an increased risk of EFS event by ctDNA burden dichotomized at 0.5% after consolidation cycle 1 using a two-sided logrank test. |
Up to 6 months after completion of planned therapy
|
|
Frequency of ctDNA clearance
Aikaikkuna: Through end of consolidation 2 cycle 2 (cycle length = 14 days)
|
Will describe (proportion and 95% confidence interval overall and stratified by study regimen) the frequency of ctDNA clearance by consolidation 2 cycle 2 among those who have ctDNA burden > 0.5% at the start of consolidation 2. |
Through end of consolidation 2 cycle 2 (cycle length = 14 days)
|
|
Frequency of ctDNA-based genetic mutations
Aikaikkuna: At diagnosis
|
Will describe (proportion and 95% confidence intervals) of genetic mutations detected in ctDNA at diagnosis. |
At diagnosis
|
|
Frequency of selected toxicities by Patient Reported Outcomes Version of Common Terminology Criteria for Adverse Events (PRO-CTCAE)
Aikaikkuna: Up to 12 months after completion of systemic therapy
|
Will be evaluated using the PRO-CTCAE. |
Up to 12 months after completion of systemic therapy
|
|
Frequency of selected toxicities by Functional Assessment of Cancer Therapy General Questionnaire (FACT-G)
Aikaikkuna: Up to 12 months after completion of systemic therapy
|
Will be evaluated using the FACT-G. |
Up to 12 months after completion of systemic therapy
|
Yhteistyökumppanit ja tutkijat
Sponsori
Tutkijat
- Päätutkija: Bhuvana A Setty, Children's Oncology Group
Opintojen ennätyspäivät
Opi tärkeimmät päivämäärät
Opiskelun aloitus (Todellinen)
Ensisijainen valmistuminen (Todellinen)
Opintojen valmistuminen (Todellinen)
Opintoihin ilmoittautumispäivät
Ensimmäinen lähetetty
Ensimmäinen toimitettu, joka täytti QC-kriteerit
Ensimmäinen Lähetetty (Todellinen)
Tutkimustietojen päivitykset
Viimeisin päivitys julkaistu (Todellinen)
Viimeisin lähetetty päivitys, joka täytti QC-kriteerit
Viimeksi vahvistettu
Lisää tietoa
Tähän tutkimukseen liittyvät termit
Muita asiaankuuluvia MeSH-ehtoja
- Neoplasmat
- Neoplasmat histologisen tyypin mukaan
- Sarkooma
- Neoplasmat, side- ja pehmytkudokset
- Osteosarkooma
- Kasvaimet, luukudos
- Kasvaimet, sidekudos
- Sarkooma, Ewing
- Orgaaniset kemikaalit
- Heterosykliset yhdisteet, 1-rengas
- Heterosykliset yhdisteet
- Heterosykliset yhdisteet, 2-rengas
- Heterosykliset yhdisteet, sulatettu rengas
- Tutkintatekniikat
- Terapeuttiset lääkkeet
- Kliiniset laboratoriotekniikat
- Diagnostiikkatekniikat ja menettelyt
- Diagnoosi
- Sytologiset tekniikat
- Sytodiagnoosi
- Hiilivety
- Hiilivedyt, sykliset
- Hiilihydraatit
- Fyysiset ilmiöt
- Camptothecin
- Alkaloidit
- Podofyllitoksiinia
- Tetrahydronaftaleenit
- Naftaleenit
- Poltisykliset aromaattiset hiilivedyt
- Hiilivedyt, aromaattiset
- Polisykliset yhdisteet
- Glukosidit
- Glykosidit
- Indolit
- Diagnostiikkatekniikat, kirurginen
- Kemian tekniikat, analyyttiset
- Spektrianalyysi
- Fosforamidi -sinapit
- Typpisinappiyhdisteet
- Sinappiyhdisteet
- Hiilivety, halogenoitu
- Fosforamidit
- Organofosforiyhdisteet
- Vinca -alkaloidit
- Secologaniinin tryptamiini -alkaloidit
- Indolialkaloidit
- Indolitsidiinit
- Indolisoija
- Antrasykliinit
- Nafthaceenit
- Aminoglykosidit
- Deoksiglukoosi
- Deoksisokerit
- Daunorubisiini
- Oksatsiinit
- Irinotekaani
- Fluorodeoksiglukoosi F18
- Syklofosfamidi
- Etoposidi
- Doksorubisiini
- Vincristine
- Ifosfamidi
- Sädehoito
- Säteily
- Biopsia
- Näytteenkäsittely
- Magneettiresonanssispektroskopia
- Kirurgiset toimenpiteet, operatiivinen
- regorafenibi
Muut tutkimustunnusnumerot
- AEWS2431
- U10CA180886 (Yhdysvaltain NIH-apuraha/sopimus)
- AEWS2431 (Muu tunniste: CTEP)
- NCI-2025-00801 (Rekisterin tunniste: CTRP (Clinical Trial Reporting Program))
- AEWS2431 (Muu tunniste: Children's Oncology Group)
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